510(k) K160798 · NHA Abutment, Implant, Dental, Endosseous
IPS e.max® Press Abutment Solutions for Viteo Base Ti
| Applicant | Ivoclar Vivadent, AG, Schaan, LI |
| Decision | Substantially Equivalent, Dec 15, 2016 |
| Received | Mar 23, 2016 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K160798
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.